Dynamics and associations of microbial community types across the human body

被引:696
作者
Ding, Tao [1 ]
Schloss, Patrick D. [1 ]
机构
[1] Univ Michigan, Dept Microbiol & Immunol, Ann Arbor, MI 48109 USA
基金
美国国家卫生研究院;
关键词
VAGINAL MICROBIOME; GUT MICROBIOME; SEX;
D O I
10.1038/nature13178
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
A primary goal of the Human Microbiome Project (HMP) was to provide a reference collection of 16S ribosomal RNA gene sequences collected from sites across the human body that would allow micro-biologists to better associate changes in the microbiome with changes in health(1). The HMP Consortium has reported the structure and function of the human microbiome in 300 healthy adults at 18 body sites from a single time point(2,3). Using additional data collected over the course of 12-18 months, we used Dirichlet multinomial mixture models(4) to partition the data into community types for each body site and made three important observations. First, there were strong associations between whether individuals had been breastfed as an infant, their gender, and their level of education with their community types at several body sites. Second, although the specific taxonomic compositions of the oral and gut microbiomes were different, the community types observed at these sites were predictive of each other. Finally, over the course of the sampling period, the community types from sites within the oral cavity were the least stable, whereas those in the vagina and gut were the most stable. Our results demonstrate that even with the considerable intra-and interpersonal variation in the human microbiome, this variation can be partitioned into community types that are predictive of each other and are probably the result of life-history characteristics. Understanding the diversity of community types and the mechanisms that result in an individual having a particular type or changing types, will allow us to use their community types to assess disease risk and to personalize therapies.
引用
收藏
页码:357 / +
页数:11
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